Evidence map›Paper›PMID 16204558›Full record

ArticleApplied and environmental microbiology2005

Production of an engineered killer peptide in Nicotiana benthamiana by using a potato virus X expression system.

Marcello Donini, Chiara Lico, Selene Baschieri, Stefania Conti, Walter Magliani, Luciano Polonelli, Eugenio Benvenuto

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Applied and environmental microbiology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.4field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Microbial Nanoparticles in Biological Plant Protection.International journal of molecular sciences · 2025
    Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Antibody Peptide based antifungal immunotherapy.Frontiers in microbiology · 2012
    Article
  8. Article
  9. Viral nanoparticles as macromolecular devices for new therapeutic and pharmaceutical approaches.International journal of physiology, pathophysiology and pharmacology · 2010
    Article
  10. Mycoviruses: future therapeutic agents of invasive fungal infections in humans?European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2010
    Review
  11. Review
  12. Article
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Marcello DoniniENEA, UTS Biotecnologie, Sezione Genetica e Genomica Vegetale, C.R. Casaccia, P.O. Box 2400, I-00100 Rome, Italy.
Chiara Lico
Selene Baschieri
Stefania Conti
Walter Magliani
Luciano Polonelli
Eugenio Benvenuto
National Agency for New Technologies, Energy and Sustainable Economic Development · ITUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The decapeptide killer peptide (KP) derived from the sequence of a single-chain, anti-idiotypic antibody acting as a functional internal image of a microbicidal, broad-spectrum yeast killer toxin (KT) was shown to exert a strong microbicidal activity against human pathogens. With the aim to exploit this peptide to confer resistance to plant pathogens, we assayed its antimicrobial activity against a broad spectrum of phytopathogenic bacteria and fungi. Synthetic KP exhibited antimicrobial activity in vitro towards Pseudomonas syringae, Erwinia carotovora, Botrytis cinerea, and Fusarium oxysporum. KP was also expressed in plants by using a Potato virus X (PVX)-derived vector as a fusion to the viral coat protein, yielding chimeric virus particles (CVPs) displaying the heterologous peptide. Purified CVPs showed enhanced antimicrobial activity against the above-mentioned plant pathogens and human pathogens such as Staphylococcus aureus and Candida albicans. Moreover, in vivo assays designed to challenge KP-expressing plants (as CVPs) with Pseudomonas syringae pv. tabaci showed enhanced resistance to bacterial attack. The results indicate that the PVX-based display system is a high-yield, rapid, and efficient method to produce and evaluate antimicrobial peptides in plants, representing a milestone for the large-scale production of high-added-value peptides through molecular farming. Moreover, KP is a promising molecule to be stably engineered in plants to confer broad-spectrum resistance to phytopathogens.

Indexed as

Anti-Bacterial AgentsAntifungal AgentsBiotechnologyCapsid ProteinsKiller Factors, YeastMicrobial Sensitivity TestsNicotianaPeptidesPlant DiseasesPlant LeavesPlants, Genetically ModifiedPotexvirusProtein EngineeringProteinsPseudomonas syringaeRecombinant Fusion ProteinsAnti-Bacterial AgentsAntifungal AgentsCapsid ProteinsKiller Factors, YeastPeptidesProteinsRecombinant Fusion Proteins

Identifiers

PMID16204558
PMCPMC1265961
OpenAlexW2114866570

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.